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Patellofemoral Pain Syndrome clinical trials

View clinical trials related to Patellofemoral Pain Syndrome.

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NCT ID: NCT02827084 Recruiting - Clinical trials for Patellofemoral Pain Syndrome

Effects of Kinesio Taping in Patellofemoral Pain

Start date: May 2016
Phase: N/A
Study type: Interventional

The study aims to analyze the immediate effects and 72 hours after application of the Kinesio Taping (KT) in the electromyographic activity of the vastus medialis oblique (VMO) and vastus lateralis (VL), the isokinetic performance of the quadriceps and referred pain of subjects with PFPS. The volunteers will be randomly assigned to one of the three groups and perform one of the protocols: control - remain at rest; KT - application of Kinesio Taping with tension in the VMO region; placebo - application of Kinesio Taping without tension, in the same region. All volunteers will be submitted to the evaluation of pain intensity, the electromyographic activity of the VMO and VL and dynamometric parameters in 3 times: before the application of KT, immediately after the application of KT and after 72h of application. Average effect estimates (differences between groups) for all variables will be calculated using the mixed model ANOVA with a significance level of 5% (p ≤ 0.05).

NCT ID: NCT02810002 Completed - Back Pain Clinical Trials

Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

Start date: August 2014
Phase: Phase 1/Phase 2
Study type: Interventional

One hundred infantry recruits will be randomly assigned to two groups. Injuries will be monitored.

NCT ID: NCT02750072 Completed - Tibial Fractures Clinical Trials

INfrapatellar Versus SUprapatellar Reamed Intramedullary Nailing for Fractures of the Tibia

INSURT
Start date: September 13, 2016
Phase: N/A
Study type: Interventional

This study will investigate the incidence and severity of anterior knee pain comparing two different approaches to tibial nail fixation; Infrapatellar versus percutaneous semi-extended suprapatellar incisions. Half the patients will be randomized to the gold standard infrapatellar approach with the other half being randomized to treatment with the percutaneous semi-extended suprapatellar approach.

NCT ID: NCT02734030 Completed - Clinical trials for Anterior Knee Pain Syndrome

Knee Extensor Muscle Properties in Young Women Symptomatic and Asymptomatic for Anterior Knee Pain

Start date: April 2015
Phase: N/A
Study type: Observational

This study aims to compare the knee extensors' mechanical, morphological and myoelectric properties between subjects affected by anterior knee pain and a healthy control group. The investigators hypothesis is that patients with anterior knee pain present a reduction in the knee extensors' mechanical, morphological and myoelectric properties due to chronic muscle inhibition produced by the syndrome. In addition, the study also aims to evaluate whether there are differences in methodology for application of the Interpolated Twitch Technique for evaluation of the quadriceps muscle inhibition by comparing the use of supramaximal electrical stimulation on the femoral nerve (gold standard) with stimulation on the motor point (new methodology) in healthy subjects and individuals affected by anterior knee pain. The investigators hypothesis is that the stimulation on the motor point is less discomfortable than on the femoral nerve and muscle inhibition results are less variable (with lower dispersion) due to such lower discomfort

NCT ID: NCT02707679 Completed - Clinical trials for Patellofemoral Pain Syndrome

Comparison of Effects of Mobilization With Movement and Kinesiotaping in Patellofemoral Pain Syndrome

Start date: May 2013
Phase: N/A
Study type: Interventional

Patellofemoral Pain Syndrome (PFPS), also known as the anterior knee pain, is one of the most common musculoskeletal disorders. Most of the patients suffer from knee pain for long time. The aim of this study was to investigate the short-term effects of Mobilization with movement and Kinesiotaping on pain, function and balance in patient with PFPS.

NCT ID: NCT02674841 Completed - Clinical trials for Patellofemoral Pain Syndrome

Live Feedback to Increase Adherence in Adolescents With Patellofemoral Pain

Start date: February 2016
Phase: N/A
Study type: Interventional

This study investigates if live feedback during home-based exercises will improve the ability to perform the exercises with the prescribed time under tension (TUT) per repetition compared with no feedback among adolescents with patellofemoral pain. The hypothesis is that adolescents who receive live feedback from BandCizer™ will have a mean TUT that is significantly closer to the prescribed TUT compared to the group not receiving feedback during the course of the intervention.

NCT ID: NCT02646579 Completed - Clinical trials for Patellofemoral Pain Syndrome

Effects of Dry Needling Using Spinal and Peripheral Sites Versus Peripheral Sites Only

Start date: October 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if dry needling both low back and extremity areas is more effective for reducing pain and improving strength, balance and functional performance among patients with chronic musculoskeletal conditions compared to dry needling of extremity areas only.

NCT ID: NCT02624245 Completed - Clinical trials for Patellofemoral Pain Syndrome

The Movement Control Training Associated With Conventional Physical Therapy is More Effective Than Conventional Physical Therapy Alone in Pain and Functional Performance?

MCTACPTMECPTA
Start date: May 2013
Phase: N/A
Study type: Interventional

Assess pain, performance function, hip and knee strength and kinematics of trunk and lower limbs during single leg hop test after movement control training associated to hip and knee muscle strengthening.

NCT ID: NCT02613247 Recruiting - Clinical trials for Patellofemoral Pain Syndrome

Intra-articular Hyaluronic Acid Injection for Therapy-resistant Patellofemoral Pain Syndrome

Start date: March 2016
Phase: Phase 2
Study type: Interventional

Patellofemoral pain syndrome (PFPS) is the most common overuse injury seen in the athletic population, particularly amongst runners. The standard of care treatment for PFPS is a comprehensive active rehabilitation program. Eighty percent of patients with PFPS report improvement in their symptoms with such a program. Unfortunately, the remaining twenty percent fail to achieve adequate symptom relief with rehabilitation alone. Considering the enormous number of individuals running for fitness, PFPS represents a significant challenge to public health as the investigators strive to encourage active living in our society. A relationship between PFPS and the development of patellofemoral osteoarthritis (PFOA) has been suggested in scientific literature. Given that intra-articular viscosupplementation (hyaluronic acid) injections have shown clinically significant symptom improvement in knee osteoarthritis, and PFPS is likely on the same spectrum, the investigators propose a trial for therapy-resistant PFPS. Hyaluronic acid is a naturally occurring molecule found in the synovial fluid of freely movable joints (such as the knee). It is believed to contribute to lubrication and cushioning in these joints. The composition of synovial fluid within arthritic joints is altered, resulting in reduced fluid viscosity and elasticity. One modern formulation of hyaluronic acid is Hylan G-F 20 (Synvisc-One, Sanofi Canada). This treatment is offered as a single injection and will be utilized in this clinical trial.

NCT ID: NCT02597673 Completed - Clinical trials for Patellofemoral Pain Syndrome

Trial of Self-managed Approaches for Patellofemoral Pain Syndrome in Active Duty

Start date: July 2015
Phase: N/A
Study type: Interventional

The overall objective of this project is to compare the three home-managed treatment regimens for PFPS: neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), and NMES combined with TENS to a standard home exercise program (HEP). Each of the three treatment arms will be supplemented by HEP and compared to a group receiving standard HEP alone. The central hypothesis is that the combination of NMES with TENS will show significantly greater improvements in muscle strength, mobility, pain, daily activity and quality of life (QOL) than HEP alone. The investigators are examining: 1) whether the three treatment regimens are significantly more efficacious than standard HEP alone in improving lower extremity muscle strength, physical activity, mobility, pain, and quality of life; 2) lower extremity muscle strength, physical activity, mobility, pain, and quality of life differ significantly across the 4 time periods; 3) is there an interaction between treatment and time in relation to lower extremity muscle strength, physical activity, mobility, pain, and quality of life.